Evidence map›Paper›PMID 41918861›Full record

ArticlePeerJ2026

Application of adaptive deep learning-based automatic segmentation in radiomics model for preoperative WHO/ISUP grading of clear cell renal cell carcinoma: a retrospective comparative study with manual segmentation.

Hongqing Zhu, Zhihui Chen, Jianbo Zhang, Moran Yang, Kangchen Gu, Wenxia Bao, Yinlai Du, Sihui Hou, Wenjun Yao

Abstract readComparative Study
In one paragraph

Article in PeerJ, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Hongqing Zhu *The Second Affiliated Hospital, Anhui Medical University, Hefei, China.
Zhihui Chen *The Second Affiliated Hospital, Anhui Medical University, Hefei, China.
Jianbo ZhangThe Second Affiliated Hospital, Anhui Medical University, Hefei, China.
Moran YangThe Second Affiliated Hospital, Anhui Medical University, Hefei, China.
Kangchen GuThe Second Affiliated Hospital, Anhui Medical University, Hefei, China.
Wenxia BaoElectronic Information Engineering, Anhui University, Hefei, China.
Yinlai DuElectronic Information Engineering, Anhui University, Hefei, China.
Sihui HouThe Second Clinical Medical School, Anhui Medical University, Hefei, China.
Wenjun YaoThe Second Affiliated Hospital, Anhui Medical University, Hefei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: To evaluate the effectiveness of different methods for segmenting tumor regions of interest in building prediction models for the World Health Organization/International Society of Urological Pathology (WHO/ISUP) grade of clear cell renal cell carcinoma (ccRCC). Materials and Methods: This retrospective single-center study analyzed computed tomography (CT) images of 405 patients (training/test cohort, 324/81) with pathologically confirmed ccRCC. Two methods were used for tumor segmentation: (1) automatic segmentation: the nnU-Net model, trained on the public KiTS19 dataset, and (2) manual segmentation. Radiomics features were extracted and selected from both automatically and manually segmented images. Support vector machine (SVM) and K-nearest neighbors were used to construct pathological grade prediction models. The segmentation accuracies of nnU-Net and manual annotation were compared. The receiver operating characteristic curve, area under the curve (AUC), accuracy, sensitivity, and specificity were used to evaluate diagnostic performance. The DeLong test was used to assess the differences between the models. Results: The average Dice similarity coefficient was 0.842 ± 0.149. Automatic segmentation was time-efficient. A total of 1,834 features were extracted from each tumor. The AutoSeg-SVM model with nine features achieved the highest diagnostic performance, with an AUC value of 0.865 (0.726-1.000), an accuracy of 79.0%, sensitivity of 85.7%, and specificity of 77.6%. Both models in the automatic segmentation group showed comparable or slightly better performance than those in the manual segmentation group, although the differences were not statistically significant. Conclusions: The nnU-Net automatic segmentation provided diagnostic efficacy comparable to manual segmentation in preoperative WHO/ISUP grade prediction for ccRCC. It significantly reduced the time required for lesion segmentation and improved workflow efficiency.

Indexed as

Carcinoma, Renal CellDeep LearningKidney NeoplasmsAgedFemaleHumansMaleMiddle AgedNeoplasm GradingRadiomicsRetrospective StudiesSupport Vector MachineTomography, X-Ray ComputedWorld Health OrganizationAutomatic segmentationClear cell renal cell carcinomaRadiomicsTumor grading predictionWorld Health Organization/International Society of Urological Pathology

Identifiers

PMID41918861
PMCPMC13034870

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.